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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06257459
Other study ID # 36137/12/22
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 1, 2023
Est. completion date December 1, 2024

Study information

Verified date February 2024
Source Tanta University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In the current study, the adult infertile patients with clinical varicoceles will be included. the patients will undergo subinguinal varicocelectomy. The patients with spermatic cord lipoma detected at the time of surgery will be enrolled and divided into 2 groups( excision group, group A and preservation group (B). semen parameters will be compared in both group at 3 and 6 months after surgery


Description:

This will be a prospective randomized study, in which adult infertile patients with clinical varicocele and oligo-athenospermia admitted to Urology department Tanta university hospital will be included and then the patients with detected spermatic cord lipoma at the time surgery will be enrolled and divided into 2 groups: GROUP A : will undergo subinguinal varicocelectomy with excision of spermatic cord lipoma GROUP B : will undergo subinguinal varicocelectomy with preservation of spermatic cord lipoma Inclusion criteria: - Adult infertile males - Clinical varicocele - oligo-asthenospermia Exclusion criteria: - Adolescent varicocele - Recurrent varicocele - Presence of inguinal hernia - Azospermic patients


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date December 1, 2024
Est. primary completion date June 1, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria: - Adult infertile males - Clinical varicocele - Semen analysis show oligo-athenospermia Exclusion Criteria: - Adolescent varicocele - Recurrent varicocele - Presence of inguinal hernia - Azospermic patients

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
subinguinal varicocelectomy
exision or preservation of spermatic cord lipoma during subinguinal varicocelectomy

Locations

Country Name City State
Egypt Ahmed Zoeir Tanta Gharbeya

Sponsors (1)

Lead Sponsor Collaborator
Tanta University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary semen parameters improvement semen analysis 3 and 6 months after surgery
Primary symptoms improvement (pain and swelling) improvement of preoperative scrotal pain and swelling was assessed 3 and 6 months after surgery
Secondary postoperative complications post-operative scrotal edema, hematoma and wound infection were assessed early after surgery and late
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